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Opposite effects of the Hsp90 inhibitor Geldanamycin: induction of apoptosis in PC12, and differentiation in N2A cells

机译:Hsp90抑制剂格尔德霉素的相反作用:诱导PC12凋亡和N2A细胞分化

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摘要

The inhibitor of the Hsp90 chaperone Geldanamycin has been reported to have several cellular effects, such as inhibition of v-src activity or destabilization of Raf-1 among others. We show now that Geldanamycin treatment induces different phenotypes in different cell lines. In PC12 cells, it triggers apoptosis, whereas in the murine neuroblastoma N2A, it induces differentiation with neurite outgrowth. Geldanamycin effects cannot be mimicked by inhibition of the c-src protein tyrosine kinases, and nerve growth factor does not protect PC12 cells from apoptosis. Mitogen-activated protein kinase activities ERK and JNK are activated differently according to cell type: in PC12 cells JNK is activated, and its inhibition abolishes apoptosis, but not ERK; in N2A cells, both ERK and JNK are activated, but with peak activities at different times.
机译:据报道,Hsp90伴侣格尔德霉素的抑制剂具有多种细胞作用,例如,抑制v-src活性或Raf-1不稳定。现在我们显示格尔德霉素治疗在不同细胞系中诱导不同的表型。在PC12细胞中,它触发细胞凋亡,而在鼠神经母细胞瘤N2A中,它诱导神经突细胞分化。格尔德霉素的作用不能通过抑制c-src蛋白酪氨酸激酶来模仿,并且神经生长因子不能保护PC12细胞免于凋亡。丝裂原激活的蛋白激酶活性ERK和JNK的激活方式因细胞类型而异:在PC12细胞中,JNK被激活,其抑制作用消除了细胞凋亡,但ERK却没有。在N2A细胞中,ERK和JNK均被激活,但在不同时间具有峰值活性。

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